University of California - San Francisco Campus and Health
I-SPY Clinical Research Coordinator
University of California - San Francisco Campus and Health, San Francisco, California, United States, 94199
I-SPY Clinical Research CoordinatorDepartment:
Surgery
Job Type:
Full Time
Job Code:
80871BR
Job SummaryThe I-SPY Program involves novel trial designs in the setting of neoadjuvant chemotherapy to accelerate the drug development process. Our goal is to introduce and rapidly test novel targeted strategies for women at high risk for recurrence, at the time of primary cancer diagnosis, rather than waiting until they develop metastatic disease. Neoadjuvant therapy allows visualization of tumor response to treatment, and thus is the ideal platform to identify mechanisms of resistance, develop diagnostic markers, and individualize therapy.
The incumbent will be the Coordinator for the multi-site I-SPY 2 TRIAL, of which UCSF is the lead site. The coordinator will be responsible for the coordination of the I-SPY 2 TRIAL, which will involve the following:
Prepare protocol applications and informed consent forms for IRB submission.
Help design flow sheets, data forms, and source documents.
Gather and interpret medical, surgical, and laboratory data regarding clinical trial/study subjects.
Apply understanding of inclusion/exclusion eligibility criteria for protocols.
Recruit, enroll, register, schedule, and retain study subjects.
Record protocol specific treatments and adverse events and assist with collection and shipment of samples.
Perform tests in the clinical research center, assist research personnel to keep patients on study schedules.
Complete study forms to submit to sponsors and/or appropriate agencies.
Collect, enter and clean data into study databases, maintaining data quality.
Assist with data analysis and preparation of reports and tables.
Attend team meetings and perform other duties as assigned.
Salary and BenefitsThe salary range for this position is $34.32 - $55.19 (Hourly Rate). To learn more about the benefits of working at UCSF, including total compensation, please visit:
UCSF Benefits .
Required Qualifications
HS graduation and sufficient experience to successfully perform the assigned duties.
Therapeutic oncology clinical trial coordinator experience.
Experience with all regulatory aspects of clinical trials.
In-depth understanding of clinical trials research.
Strong organizational skills and ability to manage multiple trials.
Knowledge of Guidelines for Good Clinical Practice (GCP).
Strong project coordination skills and experience.
Excellent interpersonal, oral, and written communication skills.
Able to work independently and lead cross-functional teams.
High degree of commitment, flexibility, motivation, and assertiveness.
Ability to work effectively in a multi-disciplinary environment.
Preferred Qualifications
BA or BS in relevant field.
1 - 2 years of phase 1/2 therapeutic oncology clinical trial coordinator experience.
Experience with electronic data capture systems.
Experience with bio-specimen collection and processing.
Experience working in breast cancer.
UCSF work experience.
Knowledge on how to collect trial data while protecting human subject safety.
About UCSFThe University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences, and excellence in patient care.
Pride ValuesUCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity, and excellence.
Equal Employment OpportunityThe University of California San Francisco is an Equal Opportunity/Affirmative Action Employer.
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Surgery
Job Type:
Full Time
Job Code:
80871BR
Job SummaryThe I-SPY Program involves novel trial designs in the setting of neoadjuvant chemotherapy to accelerate the drug development process. Our goal is to introduce and rapidly test novel targeted strategies for women at high risk for recurrence, at the time of primary cancer diagnosis, rather than waiting until they develop metastatic disease. Neoadjuvant therapy allows visualization of tumor response to treatment, and thus is the ideal platform to identify mechanisms of resistance, develop diagnostic markers, and individualize therapy.
The incumbent will be the Coordinator for the multi-site I-SPY 2 TRIAL, of which UCSF is the lead site. The coordinator will be responsible for the coordination of the I-SPY 2 TRIAL, which will involve the following:
Prepare protocol applications and informed consent forms for IRB submission.
Help design flow sheets, data forms, and source documents.
Gather and interpret medical, surgical, and laboratory data regarding clinical trial/study subjects.
Apply understanding of inclusion/exclusion eligibility criteria for protocols.
Recruit, enroll, register, schedule, and retain study subjects.
Record protocol specific treatments and adverse events and assist with collection and shipment of samples.
Perform tests in the clinical research center, assist research personnel to keep patients on study schedules.
Complete study forms to submit to sponsors and/or appropriate agencies.
Collect, enter and clean data into study databases, maintaining data quality.
Assist with data analysis and preparation of reports and tables.
Attend team meetings and perform other duties as assigned.
Salary and BenefitsThe salary range for this position is $34.32 - $55.19 (Hourly Rate). To learn more about the benefits of working at UCSF, including total compensation, please visit:
UCSF Benefits .
Required Qualifications
HS graduation and sufficient experience to successfully perform the assigned duties.
Therapeutic oncology clinical trial coordinator experience.
Experience with all regulatory aspects of clinical trials.
In-depth understanding of clinical trials research.
Strong organizational skills and ability to manage multiple trials.
Knowledge of Guidelines for Good Clinical Practice (GCP).
Strong project coordination skills and experience.
Excellent interpersonal, oral, and written communication skills.
Able to work independently and lead cross-functional teams.
High degree of commitment, flexibility, motivation, and assertiveness.
Ability to work effectively in a multi-disciplinary environment.
Preferred Qualifications
BA or BS in relevant field.
1 - 2 years of phase 1/2 therapeutic oncology clinical trial coordinator experience.
Experience with electronic data capture systems.
Experience with bio-specimen collection and processing.
Experience working in breast cancer.
UCSF work experience.
Knowledge on how to collect trial data while protecting human subject safety.
About UCSFThe University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences, and excellence in patient care.
Pride ValuesUCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity, and excellence.
Equal Employment OpportunityThe University of California San Francisco is an Equal Opportunity/Affirmative Action Employer.
#J-18808-Ljbffr